Detalhes, Ficção e radiesse

Detalhes, Ficção e radiesse

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O ultrassom microfocado Liftera nãeste somente garante fins Muito mais precisos aos pacientes, como este faz com este maior conforto possível.

The areas on either side of the chin can look hollow as volume loss causes the skin to sag along your jawline and create folds.

Patients who are using medications that can prolong bleeding, such as aspirin or warfarin, may experience increased bruising or bleeding at the injection site.

Use of RADIESSE® in the dorsum of the hand may result in significant swelling of the dorsum of the hand.

Injection in the back of the hand may result in temporary difficulty performing activities. RADIESSE® may cause nodules, bumps or lumps in the back of the hand and can last up to 1 year.

You should not use RADIESSE® or RADIESSE® (+) if you have an allergy to any component of the product, if you have a history of severe allergies, if you have a bleeding disorder, or if you are pregnant or breastfeeding. You should not use RADIESSE® (+) if you have an allergy to lidocaine or medicines like it.

Use of RADIESSE® in the dorsum of the hand may result in significant swelling of the dorsum of the hand.

Healthcare practitioners should fully familiarize themselves with the product, the product educational materials and the entire package insert.

You should minimize strenuous activity and avoid extensive sun or heat exposure for about 24 hours after treatment and until any swelling or redness has resolved.

Use of RADIESSE® liftera in the dorsum of the hand may result in significant swelling of the dorsum of the hand.

Patients who are using medications that can prolong bleeding, such as aspirin or warfarin, may experience increased bruising or bleeding at the injection sitio.

Radiesse (+) treatments of jawline contour should only be administered by providers who have appropriate training and experience and who are knowledgeable about the anatomy at and around the sitio of injection.

1 Successful completion of this indication-specific training by providers is necessary prior to their administration of fillers for such new indications.

Delayed-onset inflammation near the sitio of injection is one of the known adverse events associated with dermal fillers. Cases of delayed-onset inflammation have been reported to occur at the treatment sitio following viral or bacterial illnesses or infections, vaccinations, or dental procedures. Typically, the reported inflammation was responsive to treatment or resolved on its own.